{"@context":{"@vocab":"https://schema.org/","dcterms":"http://purl.org/dc/terms/"},"@type":"Organization","@id":"https://api.morvs.ai/medical-device-mfr/3025032529#org","identifier":[{"@type":"PropertyValue","propertyID":"FDA Establishment Identifier (FEI)","value":"3025032529"},{"@type":"PropertyValue","propertyID":"FDA Owner/Operator Number","value":"10092839"}],"name":"VIVATEC CO.,LTD.","legalName":"VIVATEC CO.,LTD.","parentOrganization":{"@type":"Organization","name":"VIVATEC Co.,Ltd.","identifier":"10092839"},"address":{"@type":"PostalAddress","streetAddress":"2-10-1,Kitahanada-cho,Kita-ku,","addressLocality":"Sakai-shi Osaka","addressRegion":null,"postalCode":"591-8002","addressCountry":"JP"},"additionalType":["Manufacture Medical Device","Manufacture Medical Device for Another Party (Contract Manufacturer)"],"additionalProperty":[{"@type":"PropertyValue","propertyID":"Mandatory US Agent","value":"Frederick Hart Co., Inc."},{"@type":"PropertyValue","propertyID":"FDA Product Codes","value":"EFW"},{"@type":"PropertyValue","propertyID":"Registration expiry year","value":"2026"}],"sameAs":["https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRL/rl.cfm?lid=3025032529"],"isAccessibleForFree":true,"license":"https://creativecommons.org/publicdomain/zero/1.0/","_source":{"data_provider":"AI Analytics","brand_name":"MORVS","brand_url":"https://morvs.ai/","data_provider_url":"https://api.morvs.ai","license":"https://creativecommons.org/publicdomain/zero/1.0/","primary_source":"https://open.fda.gov/apis/device/registrationlisting/","generated_at":"2026-11-04T12:05:23.818Z"}}